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Enrolling by invitation NCT07635030

GABA and GSH in FRDA

Observational Friedreich's Ataxia FRDA

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: MRI/ MRS (Magnetic Resonance Imaging /Magnetic Resonance Spectroscopy).
Who it may be relevant to
Registry conditions: Friedreich's Ataxia, FRDA. Basic parameters: 8 years — 16 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
United States
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

Magnetic Resonance Spectroscopy (MRS) Estimates of Glutathione (GSH) and GABA as Biomarkers of Pathophysiology in FRDA

Overview

The goal of this study is to obtain gamma-aminobutyric acid (GABA) and glutathione (GSH) assessment derived from magnetic resonance spectroscopy (MRS), to be used as a potential biomarker in patients with Friedreich Ataxia (FRDA) prior to (Aim 1), and after taking Omaveloxolone (Aim 2). Analysis will consist of: A. Comparison of values in controls with those of FRDA patients (Aim 1) B. Longitudinal comparison of values in FRDA patients repeated after Omaveloxolone administration at 3 time points (minimum of 6 months) (Aim 2) FRDA participants will be asked to complete an MRS scan at 3 timepoints in order to observe GABA and GSH activity.

Interventions

  • Other MRI/ MRS (Magnetic Resonance Imaging /Magnetic Resonance Spectroscopy)
    Subjects will undergo an MRI scan wherein the investigator will use a published, but recently developed, MRS protocol (HERMES) for simultaneous assessment of GABA and glutathione (GSH) in a single scan using a 3T MR scanner

Primary outcome measures

  • GABA Assessment [Time frame: 3 years]
  • Changes in NAA [Time frame: 3 years]
  • GSH Assessment [Time frame: 3 years]
  • Changes in MRS metabolite levels (Changes in ml) [Time frame: 3 years]

Eligibility criteria

Inclusion criteria

  • Age ≥ 8 years; <16 years
  • Written informed consent provided
  • Balletic Guanine-adenine-adenine (GAA) trinucleotide repeat length > 55 in intron 1 of Frataxin (FXN) and/or GAA repeat length > 55 in intron 1 of FXN in one allele and another type of mutation that is inferred to cause loss of function in the second FXN allele as documented in the medical record
  • Friedreich's Ataxia Rating Scale (FARS) Functional staging score of ≤ 5\^ and total modified Friedreich's Ataxia Rating Scale (mFARS) score of ≤ 65 on enrolment

Exclusion criteria

  • Age < 8 years > 16 years
  • Acute or ongoing medical or other conditions that is deemed to interfere with the conduct and assessments of the study
  • Other psychiatric or neurologic conditions apart from FRDA that, in the opinion of the Site Investigator, would interfere with the conduct and assessments of the study
  • MR contraindications (e.g., pacemaker or other metallic surgical implants)
  • Presence of metallic dental braces
  • Currently pregnant participants
  • Confined to wheelchair or bed with total dependency for all activities of daily living. Total disability.
  • Unable to understand English instruction

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Observational model
Case-control

Study locations

United States · 1 center
  • The Children's Hospital of Philadelphia — Philadelphia

Identifiers

NCT: NCT07635030 · IRB 23-021822

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗